Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP977703.RADPZENHnSIRVeZtTyxzl7VfjpwaL4SW__i0m3ttlsw-0130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP977703.RADPZENHnSIRVeZtTyxzl7VfjpwaL4SW__i0m3ttlsw-0130_assertion type Assertion NP977703.RADPZENHnSIRVeZtTyxzl7VfjpwaL4SW__i0m3ttlsw-0130_head.
- NP977703.RADPZENHnSIRVeZtTyxzl7VfjpwaL4SW__i0m3ttlsw-0130_assertion description "[LCA5, a rare genetic cause of leber congenital amaurosis in Koreans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP977703.RADPZENHnSIRVeZtTyxzl7VfjpwaL4SW__i0m3ttlsw-0130_provenance.
- NP977703.RADPZENHnSIRVeZtTyxzl7VfjpwaL4SW__i0m3ttlsw-0130_assertion evidence source_evidence_literature NP977703.RADPZENHnSIRVeZtTyxzl7VfjpwaL4SW__i0m3ttlsw-0130_provenance.
- NP977703.RADPZENHnSIRVeZtTyxzl7VfjpwaL4SW__i0m3ttlsw-0130_assertion SIO_000772 19172513 NP977703.RADPZENHnSIRVeZtTyxzl7VfjpwaL4SW__i0m3ttlsw-0130_provenance.
- NP977703.RADPZENHnSIRVeZtTyxzl7VfjpwaL4SW__i0m3ttlsw-0130_assertion wasDerivedFrom befree-20150227 NP977703.RADPZENHnSIRVeZtTyxzl7VfjpwaL4SW__i0m3ttlsw-0130_provenance.
- NP977703.RADPZENHnSIRVeZtTyxzl7VfjpwaL4SW__i0m3ttlsw-0130_assertion wasGeneratedBy ECO_0000203 NP977703.RADPZENHnSIRVeZtTyxzl7VfjpwaL4SW__i0m3ttlsw-0130_provenance.